US11202800B1ActiveUtility
Methods for treating emotional cognitive disconnect
Est. expiryFeb 26, 2033(~6.6 yrs left)· nominal 20-yr term from priority
Inventors:Jeanne Fleming
A61K 33/30A61K 33/06A61K 31/198A61K 31/047A61K 31/19
28
PatentIndex Score
0
Cited by
4
References
14
Claims
Abstract
The present invention relates to the treatment of refractory Emotional Cognitive Disconnect (ECD) through a combination of pharmaceutical agents and therapy. Individual patients are treated with a combination of magnesium, inositol, and N-acetylcysteine along with Vitamin E, Vitamin C, zinc, biotin, alphalipoic acid and lysine as required. The compositions may be administered sequentially or simultaneously in any order and may be formulated in singular or combinatorial dosage forms.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. A method of treating Emotional Cognitive Disconnect in treatment-resistant individuals, comprising:
identifying an individual suffering from Emotional Cognitive Disconnect, wherein an individual presenting with:
separation of affect/emotion and cognition,
inability to self-observe the separation and account for it,
inability to combine affects and cognitions, and
repeated inability of the individual to listen when affect/emotion and cognitions are combined by someone else,
is identified as suffering from Emotional Cognitive Disconnect;
administering daily to the individual a first composition consisting of 250 mg of magnesium per day for a first month;
evaluating the individual weekly for tolerance of the first composition;
monitoring the individual weekly for increased emotional processing, wherein increased emotional processing is a decrease in the separation of affect/emotion and cognition;
determining the tolerance for the first composition; and
while continuing administration of the first composition, sequentially administering daily a second composition comprising about 250 mg of inositol, wherein a level of inositol is increased by about 250 mg per day for a second, third, and fourth month.
2. The method of claim 1 , wherein the inositol is increased to about 18000 mg per day.
3. The method of claim 1 , further comprising sequential daily administration of a third composition comprising about 500 mg to about 1000 mg per day of N-acetylcysteine in combination with the first composition and the second composition for a fifth and sixth month.
4. The method of claim 3 , further comprising sequential administration of a fourth composition comprising about 50 mg of zinc.
5. The method of claim 4 , wherein the first, second, third, and fourth compositions are administered up to a total of 24 months.
6. The method of claim 1 , wherein the individual is evaluated by clinical observation.
7. The method of claim 1 , wherein tolerance for the first composition is determined by an absence of stomach upset, nausea, vomiting, or diarrhea.
8. A method of restoring parasympathetic functioning comprising:
identifying an individual suffering from Emotional Cognitive Disconnect, wherein an individual presenting with:
separation of affect/emotion and cognition,
inability to self-observe the separation and account for it,
inability to combine affects and cognitions, and
repeated inability of the individual to listen when affect/emotion and cognitions are combined by someone else,
is identified as suffering from Emotional Cognitive Disconnect;
administering daily to the individual in need of restoration a first composition consisting of 250 mg of magnesium for a first month;
evaluating the individual weekly for tolerance of the first composition;
monitoring the individual weekly for increased parasympathetic functioning;
determining the tolerance for the first composition; and
while continuing administration of the first composition, sequentially administering daily a second composition comprising about 250 mg of inositol, wherein a level of inositol is increased by about 250 mg per day for a second, third, and fourth month.
9. The method of claim 8 , wherein the inositol is increased to about 18000 mg per day.
10. The method of claim 8 , wherein increased parasympathetic functioning is evaluated using one or more methods selected from a Valsalva maneuver, respiratory arrhythmia, isometric handgrip test, cold pressor test, mental arithmetic, orthostatic test, mental arithmetic test, head up tilt test, baroreflex sensitivity testing, analysis of heart rate variability, measurements of noradrenaline concentration, microneurography, thermoregulatory sweat test, sympathetic skin response, and quantitative sudomotor axon reflex test.
11. The method of claim 10 , further comprising sequential daily administration of a third composition comprising about 500 mg to about 1000 mg per day of N-acetylcysteine in combination with the first composition and the second composition for a fifth and sixth month.
12. The method of claim 11 , further comprising sequential administration of a fourth composition comprising about 50 mg of zinc.
13. The method of claim 12 , wherein the first, second, third, and fourth compositions are administered up to a total of 24 months.
14. The method of claim 13 , wherein the individual is monitored by clinical observation and by using at least one clinical scale selected from a Beck Depression Inventory, or a Cage Questionnaire for the testing of Opioid Dependence of Sexual Abuse victims with chronic pain.Join the waitlist — get patent alerts
Track US11202800B1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.